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Estrad B.V.

Country not established

Devices
1

What Estrad B.V. makes

Estrad B.V. manufactures the PERIO CONTROL II, which is a dental device.

The company is based in the US, and its product is classified as a Class I device listed in the fda_510k registry.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Perio Control Ii Ref K972642

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Estrad B.V. have in the registry?

The registry currently lists 1 device for Estrad B.V.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Estrad B.V.'s devices?

Among its 1 most recently registered device, Estrad B.V. has devices listed in FDA 510(k) (1 device).

What risk classes do Estrad B.V.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Estrad B.V.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Estrad B.V. in the registry?

The most recently registered devices listed for Estrad B.V. include PERIO CONTROL II.

Generated automatically from registry data and not verified by a human reviewer.